Literature DB >> 21872597

Innate immunity and stress physiology of eastern hellbenders (Cryptobranchus alleganiensis) from two stream reaches with differing habitat quality.

William A Hopkins1, Sarah E Durant.   

Abstract

In addition to depriving amphibians of physical habitat requirements (e.g., shelter, moisture, and food), habitat modification may also have subtle effects on the health of amphibians and potentially precipitate interactions with other deleterious factors such as pathogens, contaminants, and invasive species. The current study was designed to evaluate the physiological state of imperiled giant salamanders, the eastern hellbender (Cryptobranchus alleganiensis), experiencing different surrounding land use that influences in-stream habitat quality. When we compared hellbenders from a stream reach with greater anthropogenic disturbance to a more forested site, we found that baseline and stress-induced plasma levels of corticosterone were similar in the two areas, but were very low compared to other amphibians. Males consistently had higher plasma corticosterone levels than females, a finding congruent with the known territorial activities of males early in the breeding season. Innate immune responsiveness (measured as bactericidal ability of blood; BKA) was also similar at the two sites, but juveniles had less robust BKA than adults. We found a positive relationship between restraint time and BKA, suggesting that the bactericidal ability of hellbenders may improve following acute stress. Finally, there was a tendency for hellbenders with skin abnormalities to have higher BKA compared to individuals with normal integument, an observation consistent with patterns observed in other animals actively responding to pathogens. Our study provides foundational physiological information on an imperiled amphibian species and reveals important knowledge gaps that will be important for understanding the ecology, evolution, and conservation of hellbenders.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21872597     DOI: 10.1016/j.ygcen.2011.08.006

Source DB:  PubMed          Journal:  Gen Comp Endocrinol        ISSN: 0016-6480            Impact factor:   2.822


  13 in total

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